Item Description The Accu-Chek Safe-T-Pro Uno lancing device keeps up with increased safety and hygienic requirements by health authorities, legislators, and health institutions. At the same time, it provides an ergonomic handling, lancing in just 3 milliseconds, and safety features that prevent accidental needle sticks. Its pre-set lancing depth makes it ready to use immediately. Benefits and Features Ready to use with a pre-set depth setting Safe-T-Technology ensures the needle is always safely stored away Stored needle prevents accidental needle sticks Ergonomical and easy to grip for safe handling Hygienic - each lancet can only be used once Beveled needle and small diameter for virtually pain-free blood sampling Equally suitable for right and left-handed use After a single use, the complete lancing device is disposed of Additional specifications Pre-fixed depth setting: Yes Penetration depth: 1.5 mm Needle diameter : 0.36 mm (28 G) Special needle cut: 3-facet cut Siliconized needle: Yes Sterility : 4 years after sterilization Single-use only: Yes Automatic retraction of needle : Yes Recognition of used device : Yes Intuitive handling : Yes How to use the Accu-Chek Safe-T-Pro Uno Simple, 2-step lancing Twist the sterility cap one quarter turn and remove it. Hold the lancing device between your index finger, middle finger, and thumb. Press the lancing device firmly against the chosen puncture site. Using your thumb, press the release button down completely. Move the lancing device away from the puncture site and discard it.

INTENDED USE The Finecare™ 2019-nCoV RBD Antibody Test is a fluorescence immunoassay used along with Finecare™ FIA Meters for qualitative and semi-quantitative detection of spike receptor-binding domain (RBD) antibodies of novel coronaviruses (2019-nCoV) in human fingerstick whole blood, venipuncture whole blood, serum or plasma specimen. The 2019-nCoV RBD antibodies are protective antibody produced by the human body after inoculation with 2019-nCoV vaccine or infection with 2019-nCoV. The test is intended as an aid to assess the adaptive humoral immune response to the 2019-nCoV RBD protein. STORAGE AND STABILITY 1. Store at 4~30°C in the sealed pouch up to the expiration date printed on the package. Do not freeze. 2. The test device should be used within 1 hour after taking out from the foil envelope. 3. Keep away from sunlight, moisture and heat. 4. Kit contents are stable until the expiration date printed on the outer box.

Intended Use Dengue NS1 Antigen FP is a rapid solid phase immuno- chromatographic test for the qualitative detection of Dengue NS1 Antigen in human Whole Blood/ Serum/ Plasma. This test is for in vitro diagnostic use only and is intended as an aid in the earlier diagnosis of dengue infection. Salient Features Rapid ,visual test for the qualitative detection of Dengue NS1 Antigen in whole blood/serum/Plasma. Sample can be taken from Finger prick and sample required is 4µl. Based on Sandwich principle. Detection of Dengue in Seronegative stage i.e From Day 1 of fever. Detection of all 4 serotypes of dengue virus. Reliable diagnosis of both primary and secondary infection. 100% Sensitivity & 99.96 % Specificity. Shelf life: 24 month at 2-30 °C Convenient pack Size: 10 Test. Evaluated By Referral Medical college / Hospitals /Research institutes / Labs.

Intended Use Dengue NS1 Antigen self-test is a rapid solid phase immune-chromatographic test for the qualitative detection of Dengue NS1 Ag in human whole blood/serum/plasma. This test is intended to be for home use with self-collected whole blood specimens from individuals aged 18 years or above( or collected by adults for individuals below 18 years of age) as well as for professional use with venous Whole blood/Serum/Plasma samples. This test is for in-vitro diagnostic use only & is designed as an aid in the early diagnosis of dengue infection patients with clinical symptoms. Salient Features Rapid, Visual, Home test for qualitative detection of Dengue NS1 antigen detection in human whole blood/serum/plasma. Finger prick sample can be used. Single test pack. All material to perform the test & its disposal are provided with the kit. Based on Sandwich principle.\ Detection of Dengue in Seronegative stage i.e. from Day 1 of fever. Detection of all 4 serotypes of dengue virus. Reliable diagnosis of both primary and secondary infection. 100% Sensitivity & 100 % Specificity. Shelf life: 30 month at 2-30 °C.

Intended Use Scrub Typhus IgM/IgG/IgA Card is a rapid solid phase immuno-chromatographic assay for the qualitative detection of IgM, IgG& IgA antibodies to Scrub Typhus in human serum / plasma / whole blood. This test is for in vitro diagnostic use only and is intended as an aid to early diagnosis of Scrub Typhus infection in patient with clinical symptoms. Salient Features Finger prick, rapid, visual and qualitative Immunoassay. Detection of all antibodies (IgM, IgG, IgA) to Scrub Typhus (Tsutsugamushi) in Whole blood/serum / plasma. Based on Immunochromatography Technique. See through device for easy interpretation of results. Results within 20 minutes Shelf life 30 months at 2-30°C Convenient pack size: 25 T. Sensitivity & Specificity: 100%

Intended Use HIV Ag & Ab Card (4th Generation) is a visual, rapid qualitative and sensitive solid phase immunochromatographic assay for the differential detection of HIV-1 p24 Antigen and Antibodies (IgM, IgG & IgA) to HIV-1& HIV-2 in Human Serum/ Plasma/ Whole blood (collected by venipuncture or Fingerprick). The test is a screening test for p24 antigen (HIV-1) and HIV antibodies (anti-HIV-1 & anti-HIV-2) and is for in vitro diagnostic use only. It is intended for screening of blood donors or other individuals at risk for HIV-1 & HIV-2 infection and for clinical diagnostic testing. It is a screening test for p24 antigen (HIV-1) and HIV antibodies (anti-HIV-1 & anti-HIV-2). The test is for in vitro diagnostic use only and is intended for screening of blood donors or others individuals at risk for HIV-1 and/or HIV-2 infection and for clinical diagnostic testing. Salient Features • Finger prick, rapid, visual and qualitative Immunoassay. • 4TH Generation Rapid test for differential detection of p24 Antigen & antibodies for HIV in serum/plasma /whole blood. • Ideal for Blood screening, detects sero-negative HIV Cases. • Use of gp-41, C terminus of gp120 for HIV-1 , gp-36 for HIV -2 antibodies and Anti-p24 for HIV p24 Ag detection. • Detection of Group ‘0’ & subtype ‘C’ of HIV-1, which is most prevalent in India. • Based on Immunochromatography Technique. • See through device for easy interpretation of results. • Sensitivity : 100 % & Specificity: 100% • Analytical Sensitivity of HIV p24 Ag : 100 IU/ml (traceable to p24 Antigen NIBSC Standard, U.K. Code No. 90/636) • Long Shelf life 30 months at 2-30°C • Convenient pack size: 25 T.

hemochroma PLUS is a handheld device that can run tests for anemia. One uses a disposable test cuvette to pick up sample blood from the fingertip. It accommodates tube bloods with a pipette. Each test takes 3~5 seconds and the user can transmit the result to a host computer.

Brand new BeneHeart D60 has made a major breakthrough for the industry. The multi-talent D60 integrating 12-lead ECG and POCUS, gives strong boost for on-site diagnosis. The first ever int-ext dual-factor evaluation system with closed-loop rescue approach combining resuscitation, debriefing, and training, supports continuous improvement of the rescue quality. With full touch screen and key hard buttons allowing for quick and neat control, BeneHeart D60 effectively expands rescue potential and makes rescuers more confident. Smart Touch, More Intuitive With advanced high-definition capacitive touch screen technology and flat UI design, D60 brings a clearer visual experience and more smooth operation feelings, making efficiency at your fingertips. First 9” display with 1200 x 1020 resolution Auto-brightness Gesture-control touchscreen Keep physical knob and buttons for key operations With the intelligent sensing, you can operate D60 normally, even if - the screen is spilled with liquid - wearing up to 5 layers of gloves All in one-360J Manual defib /AED /Pacing /Monitoring: ECG, SPO2, NIBP, CO2 Ultra-light Only 4.2kg (with battery) for exceptional portability Versatile paddles-External paddles with contact indicator improve usability for clinicians Visual AlarmSight™ Problem-solving support with graphical visualization One Device with Multi-talent

Product Details: Display of SpO2 % PR & plethysmogram waveform Resolution 320 x 240 pixels Certification CE 0123, FDA Type Finger Pulse Handling Portable Display LED Supporting on the capabilities of our well experienced personnel, we are providing an excellent quality array of Pulse Oximeter. Our pulse oximeter is acclaimed in the industry owing to its easy installation. This pulse oximeter is developed under the direction of skilled professionals utilizing the optimum grade component as per the set industry norms. Provided pulse oximeter is obtainable in different specifications to meet the varied needs of clients. Features: Robust Construction Perfect Finish Enhanced functional life